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Thermo Fisher Scientific MPP9 Polyclonal Antibody
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Thermo Fisher Scientific MPP9 Polyclonal Antibody

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Rabbit polyclonal antibody targeting human MPP9 (amino acids 81–126). Suitable for Western blot in human, mouse, and rat samples. High purity (>95%) and antigen affinity chromatography purified. Supplied as liquid form, unconjugated, 1 mg/mL concentrat...

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PA536981
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오후 07:06
Thermo Fisher Scientific PA536981 MPP9 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific MPP9 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to amino acids 81–126 of human MPP9
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2553848

Product Specific Information

  • Detects endogenous protein at molecular weights of 78 and 116 kDa.
  • Purity >95% by SDS-PAGE.

Target Information

Progression of cells from interphase to mitosis involves alterations in cell structures and activities. The transition from G2 to M phase is induced by M phase-promoting factor (MPF). In M phase, many proteins are phosphorylated directly by MPF or indirectly by kinases activated by MPF. These M phase phosphoproteins (MPPs), also known as MPHOSPHs, permit disassembly of interphase structures and generation of M phase enzymatic activities and structures.

MPP9 (M-phase phosphoprotein 9), also known as MPHOSPH9, is a 1,031 amino acid peripheral membrane protein of the Golgi apparatus that exists as two alternatively spliced isoforms. The gene encoding MPP9 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with various diseases, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

제품 이미지

(이미지 파일: PA5-36981_MPP9_Q99550-1_Rabbit.svg, PA5-36981_MPP9_Q99550-1_Rabbit_PDP.jpeg)

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